Safety syringe

ABSTRACT

One embodiment is directed to a safety syringe system, comprising a syringe body; a plunger tip positioned within the syringe body; a needle assembly removably coupleable to the distal end of the syringe body such that a medicinal fluid may be transferred through a retractable needle coupled to a needle housing comprising the needle assembly upon insertion of the plunger tip relative to the syringe body; and a plunger control assembly coupled to the plunger tip and configured to facilitate manual insertion of the plunger tip relative to the syringe body; wherein upon insertion and release of the plunger tip, a retraction load coupled between the syringe body and the plunger tip causes the plunger tip to be proximally withdrawn, pulling the retractable needle proximally relative to the needle housing to a safe locked and retracted state.

RELATED APPLICATION DATA

The present application claims the benefit under 35 U.S.C. §119 to U.S.provisional patent application Ser. No. 61/841,702 filed Jul. 1, 2013.The foregoing application is hereby incorporated by reference into thepresent application in its entirety.

FIELD OF THE INVENTION

The present invention relates generally to injection systems, devices,and processes for facilitating various levels of control over fluidinfusion, and more particularly to systems and methods related to safetysyringes in healthcare environments.

BACKGROUND

Millions of syringes, such as that depicted in FIG. 1A (2), are consumedin healthcare environments every day. A typical syringe (2) comprises atubular body (4), a plunger (6), and an injection needle (8). As shownin FIG. 1B, such a syringe (2) may be utilized not only to inject fluidinto a patient, but also to withdraw or expel fluid out of or into acontainer such as a medicine bottle, vial, bag, or other drugcontainment system (10). Indeed, due to regulatory constraints in somecountries such as the United States as well as sterility maintenanceconcerns, upon use of a medicine bottle (10) with a syringe (2) as shownin a particular patient's environment, such medicine bottle may only beutilized with a single patient and then must be disposed of—causingsignificant medical waste from bottle and remaining medicine disposal,and even contributing to periodic shortages of certain critical drugs.Referring to FIG. 2A, three Luer-type syringes (12) are depicted, eachhaving a Luer fitting geometry (14) disposed distally, so that they maybe coupled with other devices having similar mating geometry, such asthe Luer manifold assembly (16) depicted in FIG. 2B. The Luer fittings(14) of the syringes of FIG. 2A may be termed the “male” Luer fittings,while those of FIG. 2B (18) may be termed the “female” Luer fittings;one of the Luer interfaces may be threaded (in which case theconfiguration may be referred to as a “Luer lock” configuration) so thatthe two sides may be coupled by relative rotation, which may be combinedwith compressive loading. In other words, in one Luer lock embodiment,rotation, possibly along with compression, may be utilized to engagethreads within the male fitting which are configured to engage a flangeon the female fitting and bring the devices together into a fluid-sealedcoupling. In another embodiment, tapered interfacing geometries may beutilized to provide for a Luer engagement using compression withoutthreads or rotation (such a configuration may be referred to as a“slip-on” or “conical” Luer configuration). While such Luer couplingsare perceived to be relatively safe for operators, there is risk ofmedicine spilling/leaking and parts breakage during the loading toprovide a Luer coupling. The use of needle injection configurations, onthe other hand, carries with it the risk of a sharp needle contacting orpoking a person or structure that is not desired. For this reason,socalled “safety syringes” have been developed.

One embodiment of a safety syringe (20) is shown in FIG. 3, wherein atubular shield member (22) is spring biased to cover the needle (8) whenreleased from a locked position relative to the syringe body (4).Another embodiment of a safety syringe (24) is shown in FIGS. 4A-4B.With such a configuration, after full insertion of the plunger (6)relative to the syringe body (4), the retractable needle (26) isconfigured to retract (28) back to a safe position within the tubularbody (4), as shown in FIG. 4B. Such a configuration which is configuredto collapse upon itself may be associated with bloodspatter/aerosolization problems, the safe storage of pre-loaded energywhich may possible malfunction and activate before desirable, loss ofaccuracy in giving full-dose injections due to residual dead spacewithin the spring compression volume, and/or loss of retraction velocitycontrol which may be associated with pain and patient anxiety.

Further complicating the syringe marketplace is an increasing demand forpre-filled syringe assemblies such as that depicted in FIG. 5A, whichgenerally comprise a syringe body, or “drug enclosure containmentdelivery system”, (34), a plunger tip, plug, or stopper (36), and adistal seal or cap (35) which may be fitted over a Luer type interface.Liquid medicine may reside in the volume, or medicine reservoir, (40)between the distal seal and the distal end (37) of the plunger tip (36).Such assemblies are desirable because they may be standardized andproduced with precision in volume by the few manufacturers in the worldwho can afford to meet all of the continually changing regulations ofthe world for filling, packaging, and medicine/drug interfacingmaterials selection and component use. Such simple configurations,however, generally will not meet the new world standards for single-use,safety, auto-disabling, and anti-needle-stick. Thus certain suppliershave moved to more “vertical” solutions, such as that (41) featured inFIG. 5B, which attempts to meet all of the standards, or at least aportion thereof, with one solution; as a result of trying to meet thesestandards for many different scenarios, such products may havesignificant limitations (including some of those described above inreference to FIGS. 3-4B) and relatively high inventory and utilizationexpenses.

There is a need for improved injection systems which address theshortcomings of currently-available configurations. In particular, thereis a need for safety injection solutions which may utilize the existingand relatively well-controlled supply chain of conventionally deliveredpre-filled syringe assemblies such as that described in reference toFIG. 5A.

SUMMARY OF THE INVENTION

One embodiment is directed to a safety syringe system, comprising: asyringe body forming a fluid reservoir and having proximal and distalends; a plunger tip positioned within the fluid reservoir in aconfiguration such that medicinal fluid may be contained within thefluid reservoir; a needle assembly removably coupleable to the distalend of the syringe body such that the medicinal fluid may be transferredthrough a retractable needle coupled to a needle housing comprising theneedle assembly upon insertion of the plunger tip relative to thesyringe body; and a plunger control assembly coupled to the plunger tipand configured to facilitate manual insertion of the plunger tiprelative to the syringe body; wherein upon insertion of the plunger tipto a final insertion state and release of an associated manual insertionload, a retraction load coupled between the syringe body and the plungertip causes the plunger tip to be proximally withdrawn, pulling theretractable needle proximally relative to the needle housing to aretracted state wherein a distal tip of the needle becomes mechanicallylocked into an encapsulated configuration wherein it is no longerexposed for injection. The fluid reservoir may comprise a substantiallycylindrical volume. The syringe body may comprise a glass material. Thesyringe body may comprise a polymeric material. The plunger tip maycomprise an elastomeric material. The elastomeric material may comprisea butyl-based rubber. The needle may comprise a hypodermic needle. Thehypodermic needle may comprise a standard size between about 20 gaugeand about 34 gauge. The needle assembly may comprise a movable needleinsertion-preventing member configured to prevent re-insertion of theneedle relative to the syringe body after the needle has been placed inthe retracted state. The insertion-preventing member may be configuredto move along an axis that is substantially perpendicular to alongitudinal axis of the needle. The system further may comprise areleasing member operatively coupled to the insertion-preventing memberand configured to remove a fixing constraint from theinsertion-preventing member when the plunger tip reaches the finalinsertion state. The releasing member may comprise a push memberconfigured to be compressively loaded when the plunger tip is urged intothe final insertion state. The push member may be configured to releasea mechanical latch configured to hold the needle fixed in place relativeto the syringe body, thereby releasing the needle such that it may beproximally withdrawn into the retracted state. The mechanical latch maybe configured to interface directly with the needle. The mechanicallatch may be configured to interface with a needle interfacing memberthat is interfaced directly with the needle. The needle interfacingmember may comprise a compliant O-ring. The plunger control assembly maycomprise a plunger tip coupler member configured to be intercoupled withthe plunger tip. The plunger tip coupler may comprise one or morehelical threads configured to be inserted relative to the plunger tip tocouple the plunger tip coupler to the plunger tip. The plunger tipcoupler may be fixedly coupled to a plunger insertion member having aproximal end configured to be manually manipulated. The system furthermay comprise a plunger guiding flange through which the plungerinsertion member is inserted, the plunger guiding flange being removablycouplable to the proximal end of the syringe body. The retraction loadmay comprise a vacuum load. The retraction load may be developed by anintegrated spring member. The retraction load may be developed manually.A brake assembly may be intercoupled between the plunger guiding flangeand the plunger insertion member, the brake assembly being configured toprevent retraction of the plunger insertion member until after the firsttime it has been inserted to place the plunger tip in the finalinsertion state. The brake may be configured to reside in a braked staterelative to the plunger guiding flange until the plunger insertionmember is utilized to place the plunger tip in the final insertionstate, after which the brake may be configured to mechanicallytransition to an unbraked state relative to the plunger guiding flangewherein it is configured to allow the plunger insertion member to beretracted away from the syringe body.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1-5B illustrate various aspects of conventional injection syringeconfigurations.

FIGS. 6-10K illustrate various aspects of a safety syringe configurationin accordance with the present invention.

FIG. 11 illustrates a process for conducting an injection procedureutilizing a safety syringe configuration such as that described inreference to FIGS. 6-10K.

FIGS. 12A-12G illustrate various aspects of a safety syringeconfiguration in accordance with the present invention.

FIG. 13 illustrates a process for conducting an injection procedureutilizing a safety syringe configuration such as that described inreference to FIGS. 12A-12G.

FIGS. 14A-14G illustrate various aspects of a safety syringeconfiguration in accordance with the present invention.

FIG. 15 illustrates a process for conducting an injection procedureutilizing a safety syringe configuration such as that described inreference to FIGS. 14A-14G.

FIGS. 16A-16H illustrate various aspects of a safety syringeconfiguration in accordance with the present invention.

FIG. 17 illustrates a process for conducting an injection procedureutilizing a safety syringe configuration such as that described inreference to FIGS. 16A-16H.

FIGS. 18A-18I illustrate various aspects of a safety syringeconfiguration in accordance with the present invention.

FIG. 19 illustrates a process for conducting an injection procedureutilizing a safety syringe configuration such as that described inreference to FIGS. 18A-18I.

FIGS. 20A-20I illustrate various aspects of a safety syringeconfiguration in accordance with the present invention.

FIG. 21 illustrates a process for conducting an injection procedureutilizing a safety syringe configuration such as that described inreference to FIGS. 20A-20I.

FIGS. 22A-22K illustrate various aspects of a safety syringeconfiguration in accordance with the present invention.

FIG. 23 illustrates various aspects of a safety syringe configuration inaccordance with the present invention.

FIG. 24 illustrates various aspects of a safety syringe configuration inaccordance with the present invention.

DETAILED DESCRIPTION

Referring to FIG. 6, a disassembled view of a safety syringe assembly isillustrated, comprising a needle assembly (32) which may be removablycoupled to an off-the-shelf syringe body (34) forming a reservoir (40)which may be at least partially pre-filled with a fluid such as a liquidmedicine product. The distal end of the syringe body is configured tohave a Luer type coupling interface (42), while the proximal end of thesyringe body comprises a conventional syringe flange (38), such as thatknown as a “Gerresheimer” flange configuration. The syringe body (34)preferably comprises a translucent material such as a glass or polymer.To form a contained volume within the reservoir (40), and to assist withexpulsion of the associated fluid through the needle, a plunger tip (36)may be positioned within the syringe body (34). The syringe body maydefine a substantially cylindrical shape (i.e., so that a plunger tip 36having a circular cross sectional shape may establish a seal against thesyringe body), or be configured to have other cross sectional shapes,such as an ellipse. A plunger control assembly (44) is configured to becoupled to the syringe body and to engage the plunger tip (36) to assistin expelling fluid from the syringe through the needle and inwithdrawing the needle, as described below. As described above, thesyringe body flange (38) may comprise a conventional flanged geometrywhich may be selected from the syringe body supplier; preferably theplunger control assembly (44) may be configured to be coupleable to manyof the conventionally-available flange (38) geometries, such as varioussizes of the flanges available from suppliers such as Gerresheimer, asnoted above. The plunger tip (36) may comprise a standard butyl rubbermaterial and may be coated, such as with a biocompatible lubriciouscoating, to facilitate preferred sealing and relative motioncharacteristics against the associated syringe body structure andmaterial.

Referring to FIG. 7A, an exploded orthogonal view of an embodiment of aneedle assembly (32) is illustrated showing a needle cover (46)configured to form a cover or shield over at least the distal end of theneedle (58) when assembled. A distal needle housing member (48) andproximal needle housing member (50) assist in maintaining the positionof the needle relative to the syringe body, and in controlling movementof a latch mechanism that comprises a two-fingered latch member (54)movably coupled to a movable needle insertion preventing member (56).The needle member has a sharpened distal end (58) configured to beinserted in a hypodermic fashion into a tissue structure of a patient; aproximal end (60) comprises a proximal tip interface (62) that may beconfigured to stab into and couple to a portion of an associated plungertip, in a fashion that somewhat mimics the function of a harpooninstrument.

Referring to FIG. 7A, an exploded orthogonal view of an embodiment of aplunger control assembly (44) is illustrated showing a plunger insertionmember (74) intercoupling a distally-disposed plunger tip coupler member(64), which may have outer helical threads configured to “screw into”and couple to the compliant material of an associated plunger tip asdesired, a plunger insertion member proximal manipulation interface(76), a brake member (68), and a sealing flange assembly (66) comprisinga flange member (72) configured to be removably coupled to the proximalflange fitting of a conventional syringe body (such as that shown inFIG. 6 as element 38) to hold into place a syringe body proximal plugmember (88) with an additional sealing interface comprising an O-ring(70) to facilitate the buildup of a vacuum load when an associatedplunger tip is inserted relative to the sealing flange assembly (88).The plunger insertion member proximal manipulation interface (76)preferably is shaped to allow for finger and/or thumb manipulation in amanner akin to that associated with operation of a conventional syringe(i.e., depression with a thumb or finger while one or more otherfingers/digits are utilized to apply a counterload at the flange area).FIG. 8 illustrates a partially assembled configuration wherein a syringebody has been coupled to a plunger control assembly (44) with theplunger tip coupler member (64) helically advanced and coupled into theproximal aspect of the compliant plunger tip (36), and the flange member(72) coupled to the proximal flanged aspect of the syringe body (34).The needle cover (46) preferably is configured to shield/cover not onlythe distal aspect of the needle member (58), but also the proximalaspect (60, 62), in the depicted configuration, as shown, to enable anoperator to manually grasp the needle assembly (32) as shown and coupleit to the distal aspect of the syringe body (34) without placing theoperator's fingers at risk for an accidental needle puncturing.

Referring to FIG. 9A, the fairly large overlap between the distal end(80) of the syringe body outer diameter and the interfacing end (78) ofthe needle cover provides a relatively large geometric guidance surfacefor aligning the needle proximal end (60) as it is guided through theneedle assembly components during assembly/coupling with the syringebody (34) and guided into fluidic contact with the fluid reservoir ofthe syringe body (34).

Referring to FIG. 9B, a flange member (72) is shown in relation to anintercoupled syringe body (34) and plunger insertion member (74). In thedepicted embodiment, the mechanical interface between the plungerinsertion member (74) and the flange member (72) is a brake member orbrake assembly (68) which is configured to be snap-fitted into a recessformed into the flange member (72). FIG. 9C illustrates an opposingorthogonal view. FIG. 9D illustrates a flange member (72) without thebrake member in place to show the recess surface (86) formed into theflange member (72). FIG. 9E shows a brake member (68) having two outermounting release tabs (82) and two inner braking tabs (84). In thisembodiment, the brake member (68) is configured to be snapped into theflange member recess (86) and held in place by geometric featurescoupled to the outer mounting release tabs (82). In such a position, thetwo inner braking tabs (84) are geometrically biased toward the distalend of the syringe body so that they will easily cantilever away from aninserted (i.e., inserted through the two inner braking tabs 84) plungerinsertion member (element 74 in other drawings; not shown in FIGS. 9Dand 9E) during such insertion with relatively low friction—but alsoresist retraction of the same plunger insertion member with relativelyhigh loads until released from the coupling to the flange member (72).Such a release may be accomplished by depressing the two outer mountingrelease tabs (82)—and, indeed, these tabs (82) are configured to beautomatically depressed for such a release upon full insertion of theplunger insertion member to a final insertion state wherein theassociated plunger tip is interfaced against the end of the syringe andwherein the plunger insertion member proximal interface (element 76 inFIG. 7B, for example) is interfaced against the outer mounting releasetabs (82) such that they are released, and the braking member (68) isallowed to travel along with the plunger insertion member, as shown inFIG. 10I, without further resisting retraction of the associated plungerinsertion member.

Referring to FIG. 10A-10K, various operational aspects of one embodimentof a safety syringe configuration in accordance with the presentinvention are illustrated. Referring to FIG. 10A, with a needle assemblycoupled to a syringe body (34), the protective needle cover (46) may beremoved as shown to expose the distal portion of the needle (58) forinjection into a tissue structure of a patient. The internal supportmechanisms of the needle assembly may be configured to support aninjection load of about 5 pounds without yielding or slipping—to meet astandard such as those promulgated by organizations such as ISO. In thedepicted embodiment, the proximal end (60) of the needle is configuredto extend into the fluid reservoir (40) of the syringe body to become afluid conduit for injection into a tissue structure that may betemporarily interfaced with a distal portion (58) of the needle. Theneedle is threaded through a movable needle insertion preventing member(56) which imparts only very minimal frictional loads to the needle inthe depicted configuration wherein the needle is threaded directlythrough the needle insertion preventing member (56). Referring to theclose-up view of FIG. 10B, with full insertion of the plunger tip to afinal insertion state, the plunger is configured to impart a compressiveload upon the needle and/or a sleeve coupled thereto, to urge themovable needle insertion preventing member (56) against the two fingersof the clip or latch member (54), thereby urging them away from eachother (90). The geometry and structural moduli of these structures maybe configured such that upon full insertion of the plunger tip to afinal insertion state, a geometric step (element 110 as illustrated inFIG. 10C) of the movable needle insertion preventing member (56) ispushed past the two fingers of the latch member (54) so that the movableneedle insertion preventing member (56) is stuck in a position, byvirtue of the ramp surfaces (element 108 as illustrated in FIG. 10C),wherein it will remain biased open—and also biased to move in adirection (parallel to the axis 96 illustrated in FIG. 10D)substantially perpendicular to the longitudinal axis of the needle(element 98 in FIG. 10D, for example) if freed from the constraint ofthe needle passing through it. The movable needle insertion preventingmember (56) may be slidably interfaced against, and retained by in theaxial direction parallel to the longitudinal axis of the needle (98), awall (112) formed in the distal needle housing member (48), as shown inFIG. 10D. With the two fingers of the latch member (54) biased open, aneedle axial position constraining step (102) formed in the needleand/or a sleeve coupled to the needle may be freed from the constraintof the latch member (54) and allowed to retract, as shown in FIG. 10D,wherein the two latch contact points (92, 94) have been pulled apartenough that the needle is being withdrawn, here by vacuum load built upwithin the proximal aspect of the syringe body during insertion of theplunger tip. FIGS. 10E and 10F illustrate sequential images wherein themovable needle insertion preventing member (56) has been pushed past thetwo latch member (54) fingers to leave them permanently relatively opento that the needle may be retracted. Referring to FIG. 10G, withsufficient retraction of the needle so that the needle tip (58) is nolonger threaded through a first needle through-aperture (104) andconstraining the motion of the movable needle insertion preventingmember (56), the movable needle insertion preventing member (56) isurged by compressive loading of the latch member (54) fingers on theramped geometry of the movable needle insertion preventing member (56)to move along the depicted axis (96) which is substantiallyperpendicular to the needle longitudinal axis (98), thereby placing theneedle distal tip (58) in alignment with the partial-depth needleaperture (106), which is configured to specifically block and constrainthe needle distal tip (58) as a successive attempt is made to try toinsert the needle. FIGS. 10H-10J illustrate various aspects of theplunger control assembly in relation to the syringe body (34). Referringto FIG. 10k , upon full retraction of the needle into the body of thesyringe (34), the needle may be allowed to rest, or be biased to rest,in a canted or intentionally misaligned position relative to the syringebody (34) to prevent re-insertion of the needle relative to the syringebody (34). In use, the embodiments featured in FIGS. 10A-10K mayfunction as follows: an off-the-shelf pre-filled syringe body, such asthat described in reference to FIG. 5A, may be coupled to a plungercontrol assembly and needle assembly near the intended use location; theprotective needle cover may be removed, and the patient injected withthe needle, followed by insertion of the plunger tip to expel thesyringe fluid into the patient; as the plunger tip is seated into thedistal end of the syringe body, several events are intended to occur: a)the proximal end of the needle is harpooned into the plunger tip tocouple these two structures; b) a plunger retraction brake is releasedby interfacing of the plunger insertion member proximal interface andbrake member outer tabs so that the plunger insertion member andintercoupled plunger tip and harpooned needle may be withdrawn relativeto the syringe body; c) a vacuum load is maintained by a substantiallysealed proximal volume between the flange assembly (66) and the plungertip which is expanded as the plunger tip is inserted; d) a movableneedle retraction-preventing member (56) urges open the fingers of theassociated latch member (54) to allow the needle to become relativelyunconstrained in terms of proximal retraction or withdrawal into/towardthe syringe body—and upon enough retraction of the needle (i.e. via thevacuum load pulling the plunger tip, which is harpoon-coupled to theneedle so that the needle is pulled along proximally into retraction),the movable needle retraction-preventing member (56) moves over to blockfurther re-insertion of the needle tip. Thus a single-use safety syringeconfiguration is described wherein a single injecting insertion is maderelatively simple, while various mechanisms interact to allow for acontrolled retraction of the needle and prevention of re-insertion afterretraction. During the injecting insertion, the braking member of theplunger control assembly allows an operator to remove his handscompletely from the system while the brake retains the position of theplunger tip relative to the syringe body. The braking member also may beeffective in retaining the geometric relationship between a plunger tipand an associated syringe body and captured pre-filled medicine volumeduring shipping and handling before utilization. For example, withconventional configurations, such as that shown in FIG. 5A, it ispossible that changes in pressure, such as those created with airtransport, may move the plunger tip relative to the syringebody—possibly past the acceptable sterile geometric boundaries/barriers.Such relative motion may be prevented with a locking/brakingconfiguration as described herein.

Referring to FIG. 11, a process is illustrated for using an embodimentsuch as that described in reference to FIGS. 10A-10K. After preoperativediagnostics and patient preparation (200), an safety syringe injectionassembly may be assembled (202). When an injection is desired, theprotective needle cover may be removed (204) and the injection performedupon a tissue structure of the patient (206, 208). After the plunger tiphas reached a final insertion state, the built up vacuum load may beutilized to assist in withdrawing the plunger tip proximally to aretracted state (210); such insertion to the final insertion state andsubsequent retraction of the needle may cause movement of the movableneedle insertion-preventing member to move into a configuration whereinit will prevent re-insertion of the needle (212); insertion of theplunger tip to the final insertion state also causes the plunger brakingmember to mechanically transition to an un-braked state wherein plungerretraction is not mechanically resisted by the brake (214). Theretracted needle may be fully retracted into the syringe body andpositioned in a canted configuration to prevent further insertion (216).

Referring to FIGS. 12A-12G, another embodiment is depicted wherein amechanism is configured to allow for a full injection insertion, afterwhich the needle may be automatically withdrawn, and in certainembodiments, also prevented from re-insertion. For simplicity ofillustration, braking features, such as those described in reference toFIGS. 9A-10K, are not shown in the embodiments of FIGS. 12A-12G, butthey may be present in certain variations and configurations, and aredescribed, for example, in the embodiment of FIG. 13.

Referring to FIGS. 12A-12G, a safety syringe assembly is depictedwherein a needle housing (120) may be coupled to a conventional syringebody (34) and utilized to facilitate a single full insertion of theneedle, after which needle withdrawal may be automatically facilitatedby a combination of a withdrawal-prevention mechanism converting to astate wherein needle withdrawal is freely allowed, and a vacuum loaddeveloped in the captured volume proximal to the plunger tip in thesyringe body being allowed to facilitate needle withdrawal, as describedabove. As shown in FIG. 12A, a plunger tip (36) is shown ready to injectthe contents of the syringe body (34) into the needle, the distalportion (58) of which may be directly interfaced with a patient tissuestructure. Referring to FIG. 12B, a close-up view of which is shown inFIG. 12D, with the plunger tip (36) almost fully inserted, the needleremains locked in place and prevented from withdrawal by a lockingconfiguration comprising an O-ring forcibly urged against a needlesleeve (126) coupled to the needle. The proximal needle end (60)features a harpoon-like interface (64) configured to stab into theplunger tip (36) material and couple thereto. The depicted embodimentalso features a polymeric backing (122) of the plunger tip (36) selectedto create a more robust coupling of the needle and plunger tip.Referring to FIG. 12C, a close-up view of which is shown in FIG. 12E,with complete insertion of the plunger tip (36), the needle sleeve (126)urges a load-transferring member (128) at least partway through aplurality of latch members (130, 131), which rotate (132) as shown inFIG. 12E, to release an O-ring loading member (134) from its priorconstraint up against the O-ring (170), allowing the O-ring to slightlyrelax and thereby free the needle of the previous axial withdrawalconstraint, after which retraction of the plunger insertion member (74),such as by vacuum load or manually, will pull the needle into proximalwithdrawal relative to the syringe body (34), as shown in FIGS. 12F and12G.

Referring to FIG. 13, an embodiment similar to that of FIG. 11 isillustrated, with the exception that in the embodiment of FIG. 13, afterthe injection insertion (208), insertion to a final insertion statereleases compression of an O-ring from against the needle, therebyallowing the needle to be withdrawn (218), as described above inreference to FIGS. 12A-12G.

Referring to FIGS. 14A-14G, an embodiment similar to that of FIGS.12A-12G is illustrated, with the exception that the embodiment of FIGS.14A-14G features an off-axis or bent proximal harpooning or barbinterface (136) that is configured to cause a fully-withdrawn needle tobe canted to the side, or out of alignment relative to the syringe body(34), so that the needle cannot be re-inserted by another attemptedinsertion of the plunger tip. FIG. 15, which is similar to FIG. 13,features the addition of such misalignment of the needle member uponfull withdrawal of the needle member into the syringe body (220) toprevent re-insertion of the needle member relative to the syringe body(i.e., to prevent re-use, or accidental/undesired contact of a needletip with a person or object).

Referring to FIGS. 16A-16H, an embodiment similar to that of FIGS.12A-12G is illustrated, with the exception that the embodiment of FIGS.16A-16H features double off-axis or bent proximal harpooning or barbinterface (138) that is configured to cause a fully-withdrawn needle tobe canted to the side, or out of alignment relative to the syringe body(34), so that the needle cannot be re-inserted by another attemptedinsertion of the plunger tip—and also to provide an even more robustharpoon-style coupling between the proximal portion of the needle (60)and the plunger tip (36). FIG. 17, which is similar to FIG. 13, featuresthe addition of such misalignment of the needle member upon fullwithdrawal of the needle member into the syringe body using the twincoupling member (222) to prevent re-insertion of the needle memberrelative to the syringe body (i.e., to prevent re-use, oraccidental/undesired contact of a needle tip with a person or object).

Referring to FIGS. 18A-18I, an embodiment similar to that of FIGS.12A-12G is illustrated, with the exception that the embodiment of FIGS.18A-18I features a quite different mechanism for allowing insertion ofthe needle and resisting retraction until full insertion of the needle,after which retraction of the needle is facilitated by deformation of aclip member (140). For example, referring to the close-up views of FIGS.18D and 18E, in FIG. 18D, a close-up view of the configuration of FIG.18A, the clip member (140), with two through-apertures (142, 144) thatare slightly out of alignment, prevents movement of the needle (58)relative to the syringe body (34). FIG. 18E shows the plunger tip almostfully, but not fully, inserted relative to the syringe body, as in FIG.18B. Upon full insertion of the plunger tip (36), as in FIGS. 18C and18F, a needle sleeve member, or a step formed in the outer geometry ofthe needle, compresses the clip member (140), causing the apertures(142, 144) to become more aligned, if not completely aligned, afterwhich they may be held in such configuration by a feature (148) formedinto the needle housing (120) configured to retain such configuration sothat the needle may be withdrawn, such as by a manually applied load orvacuum load, as described above. In other words, the clip member (140)may be squeezed by virtue of a physical coupling through the needleassembly to the plunger tip (36), causing deformation (which may beconfigured to be plastic deformation or elastic deformation, dependingupon the materials and dimensions selected for the clip; in an elasticdeformation configuration, the holding feature 148 assists moreprominently in retaining the deformed shape of the clip) of the clip(140) to a shape such as that shown in FIG. 18F, wherein the needle (58)is allowed to retract without substantial resistance from the clip, dueto alignment of the apertures of the clip. FIG. 18H shows an incompletewithdrawal of the needle into the syringe body; FIG. 18I shows acomplete withdrawal of the needle into the syringe body, with canting ofthe withdrawn needle to the side to prevent further insertion of theneedle relative to the syringe body, as described above. The embodimentof FIG. 19 is similar to that of FIG. 15, with the exception that theembodiment of FIG. 19 features deformation of a needle retractionresistance clip, thereby allowing the needle to be withdrawn (224).

Referring to FIGS. 20A-20I, an embodiment similar to that of FIGS.12A-12G is illustrated, with the exception that the embodiment of FIGS.20A-20I features a quite different mechanism for resisting needleretraction until full insertion of the needle, after which retraction ofthe needle is facilitated by movement of a cantilevered latch member(152) of a latch assembly (150) coupled to the distal needle housing(120). For example, referring to the close-up views of FIGS. 20D and20E, in FIG. 20D, a close-up view of the configuration of FIG. 20A, thelatch member (152) prevents withdrawal of the of the needle (58)relative to the syringe body (34) by interfacing with a recess (154)formed into the needle or a sleeve member coupled thereto. FIG. 20Eshows the plunger tip almost fully, but not fully, inserted relative tothe syringe body, as in FIG. 20B. Upon full insertion of the plunger tip(36), as in FIGS. 20C and 20F, the needle and/or needle sleeve (156)member is advanced slightly forward, dislodging the latch member (152)from the recess (154), after which the needle may be withdrawn (such asis shown in FIG. 20G), such as by a manually applied load or vacuumload, as described above. FIG. 20H shows an incomplete withdrawal of theneedle into the syringe body; FIG. 20I shows a complete withdrawal ofthe needle into the syringe body, with canting of the withdrawn needleto the side to prevent further insertion of the needle relative to thesyringe body, as described above. The embodiment of FIG. 21 is similarto that of FIG. 19, with the exception that the embodiment of FIG. 21features mechanical reconfiguration of a needle retraction resistancelatch, thereby allowing the needle to be withdrawn (226).

Referring to FIGS. 22A-22K, an embodiment is depicted wherein a needleassembly features a proximally disposed intercoupling member (160)configured to be coupled (via relative rotation) to a distal Luerfitting (14) of a conventional syringe assembly, and also configured tobe coupled (also via relative rotation—preferably the same rotationaldirection as the first rotation) to an inner surface of the needlehousing (166) in a manner wherein the proximal aspect (60, 64) of theneedle remain shielded from the hands of an operator, or from otherobjects. Referring to FIG. 22A, the needle assembly comprises a needlecoupled through a needle housing (166) and intercoupled intercouplingmember (160) so that the proximal end of the needle (60, 64) does notextend beyond the proximal end of the intercoupling member (160). Aremovable needle shield (158) isolates the distal portion (58) of theneedle and is removable at injection time; further, the removable needleshield (158) features rotational manipulation features, such as smallwing features, to facilitate easy rotation of the needle assemblyrelative to the syringe body (34) to which it is to be coupled. Suchfeatures may be particularly useful for the home healthcare marketwherein patients suffering from maladies such as arthritis may desire touse syringes for injection and have difficulty without physical featureaids. Referring to FIG. 22B, the syringe assembly and needle assemblyare placed into contact with the Luer interface of the intercouplingmember (160) positioned against the Luer interface of the syringeassembly. With twisting engagement, the intercoupling begins via theintercoupling member (160), as shown in the cross sectional view of FIG.22C. With further twisting, the proximal coupling interface (164) of theintercoupling member (160) causes closer engagement of the intercouplingmember (160) using the inner helical thread interface (168) of theneedle housing—until the coupling is complete, as shown in FIGS. 22D and22E. Subsequently the removable needle shield (158) may be removed andan injection of fluid started, as shown in FIGS. 22F and 22G. Upon fullinsertion of the plunger tip (36) relative to the syringe body (34), theproximal needle harpooning interface (64) may be coupled to the plungertip (36), and an un-latching configuration similar to that shown inreference to FIGS. 20A-20I may allow for proximal withdrawal of theneedle, as shown in FIGS. 22I-22K.

Referring to FIG. 23, a configuration similar to that depicted in FIG.12A is illustrated, with exception that the configuration of FIG. 23features an integrated spring member (51) intercoupled between theneedle member (58) and the distal end of the syringe body (34) toprovide a needle retraction load sufficient to retract the needle, asdescribed above—but in the context of a vacuum retraction load.

Referring to FIG. 24, a configuration similar to that depicted in FIG.12A is illustrated, with exception that the configuration of FIG. 23features an integrated spring member (101) intercoupled between theproximal end (38) of the syringe body (34) and the proximal end of theplunger insertion member (74) to provide a needle retraction loadsufficient to retract the needle, as described above—but in the contextof a vacuum retraction load.

FIGS. 23 and 24 illustrate that loads other than vacuum loads may beutilized to assist in retracting a needle member with various safetyconfigurations described herein. Indeed, in simplified configurations,which may be desirable from cost and other perspectives, needlere-insertion prevention may be accomplished using needle assemblies suchas those described herein, with only manual retraction of the needlemember (i.e., while various self-retracting-after-full-insertionconfigurations are described herein, manual retraction configurationsalso may benefit from the safety provided by the needle assembliesdescribed herein wherein re-insertion of a needle after a first fullinsertion is physically prevented).

Referring back to FIGS. 11, 13, 15, 19, and 21, the syringe body(preloaded with medicine), needle assembly, and plunger control assemblyare illustrated (202) as being part of an in-situ process (i.e.,adjacent the point of use—such as in a hospital or home healthcarescenario, and after preoperative diagnostics and patient preparation200). In other embodiments, a plunger control assembly such as thatillustrated in FIGS. 6 and 7B (44) may arrive at the intervention sitepre-assembled with a syringe body (i.e., such an assembly would bepre-assembled before delivery to the intervention site); further, inother embodiments, a needle assembly such as that illustrated in FIGS. 6and 7A (32) may arrive at the intervention site pre-assembled with asyringe body (i.e., such an assembly would be pre-assembled beforedelivery to the intervention site); indeed, in other embodiments, both aneedle assembly (32) and plunger control assembly (44) may bepre-assembled with a syringe body at the preparation factory or otherlocation before delivery to the intervention site.

Suitable polymeric materials for the various components of theseembodiments include but are not limited to acetal, polycarbonate, polyvinyl chloride, polypropylene, polystyrene, ABS, nylon, glass-fillednylon, glass-filled acetal, peek, glass-filled peek, carbon-fiber-filledpeek, COC (cyclic olefin copolymer), COP (cyclic olefin polymer), PEI(Ultem), glass-filled PEI, and pekk, as well as copolymers thereof.

Suitable structural metals for structures such as the plunger insertionmember include but are not limited to stainless steel, steel with chromecoating, brass, nickel, and titanium, as well as alloys thereof.

Suitable needle member sizes range from about 34 gauge/6 millimeterslong—to about 20 gauge/2.5 inches long.

Various exemplary embodiments of the invention are described herein.Reference is made to these examples in a non-limiting sense. They areprovided to illustrate more broadly applicable aspects of the invention.Various changes may be made to the invention described and equivalentsmay be substituted without departing from the true spirit and scope ofthe invention. In addition, many modifications may be made to adapt aparticular situation, material, composition of matter, process, processact(s) or step(s) to the objective(s), spirit or scope of the presentinvention. Further, as will be appreciated by those with skill in theart that each of the individual variations described and illustratedherein has discrete components and features which may be readilyseparated from or combined with the features of any of the other severalembodiments without departing from the scope or spirit of the presentinventions. All such modifications are intended to be within the scopeof claims associated with this disclosure.

Any of the devices described for carrying out the subject diagnostic orinterventional procedures may be provided in packaged combination foruse in executing such interventions. These supply “kits” may furtherinclude instructions for use and be packaged in sterile trays orcontainers as commonly employed for such purposes.

The invention includes methods that may be performed using the subjectdevices. The methods may comprise the act of providing such a suitabledevice. Such provision may be performed by the end user. In other words,the “providing” act merely requires the end user obtain, access,approach, position, set-up, activate, power-up or otherwise act toprovide the requisite device in the subject method. Methods recitedherein may be carried out in any order of the recited events which islogically possible, as well as in the recited order of events.

Exemplary aspects of the invention, together with details regardingmaterial selection and manufacture have been set forth above. As forother details of the present invention, these may be appreciated inconnection with the above-referenced patents and publications as well asgenerally known or appreciated by those with skill in the art. Forexample, one with skill in the art will appreciate that one or morelubricious coatings (e.g., hydrophilic polymers such aspolyvinylpyrrolidone-based compositions, fluoropolymers such astetrafluoroethylene, hydrophilic gel or silicones) may be used inconnection with various portions of the devices, such as relativelylarge interfacial surfaces of movably coupled parts, if desired, forexample, to facilitate low friction manipulation or advancement of suchobjects relative to other portions of the instrumentation or nearbytissue structures. The same may hold true with respect to method-basedaspects of the invention in terms of additional acts as commonly orlogically employed.

In addition, though the invention has been described in reference toseveral examples optionally incorporating various features, theinvention is not to be limited to that which is described or indicatedas contemplated with respect to each variation of the invention. Variouschanges may be made to the invention described and equivalents (whetherrecited herein or not included for the sake of some brevity) may besubstituted without departing from the true spirit and scope of theinvention. In addition, where a range of values is provided, it isunderstood that every intervening value, between the upper and lowerlimit of that range and any other stated or intervening value in thatstated range, is encompassed within the invention.

Also, it is contemplated that any optional feature of the inventivevariations described may be set forth and claimed independently, or incombination with any one or more of the features described herein.Reference to a singular item, includes the possibility that there areplural of the same items present. More specifically, as used herein andin claims associated hereto, the singular forms “a,” “an,” “said,” and“the” include plural referents unless the specifically stated otherwise.In other words, use of the articles allow for “at least one” of thesubject item in the description above as well as claims associated withthis disclosure. It is further noted that such claims may be drafted toexclude any optional element. As such, this statement is intended toserve as antecedent basis for use of such exclusive terminology as“solely,” “only” and the like in connection with the recitation of claimelements, or use of a “negative” limitation.

Without the use of such exclusive terminology, the term “comprising” inclaims associated with this disclosure shall allow for the inclusion ofany additional element—irrespective of whether a given number ofelements are enumerated in such claims, or the addition of a featurecould be regarded as transforming the nature of an element set forth insuch claims. Except as specifically defined herein, all technical andscientific terms used herein are to be given as broad a commonlyunderstood meaning as possible while maintaining claim validity.

The breadth of the present invention is not to be limited to theexamples provided and/or the subject specification, but rather only bythe scope of claim language associated with this disclosure.

The invention claimed is:
 1. A safety syringe system, comprising: asyringe body forming a fluid reservoir and having proximal and distalends; a plunger tip positioned within the fluid reservoir in aconfiguration such that medicinal fluid may be contained within thefluid reservoir; a needle assembly removably coupleable to the distalend of the syringe body such that the medicinal fluid may be transferredthrough a retractable needle coupled to a needle housing comprising theneedle assembly upon insertion of the plunger tip relative to thesyringe body, wherein the needle assembly comprises a movable needleinsertion-preventing member; a plunger control assembly coupled to theplunger tip and configured to facilitate manual insertion of the plungertip relative to the syringe body, wherein upon insertion of the plungertip to a final insertion state and release of an associated manualinsertion load, a retraction load coupled between the syringe body andthe plunger tip causes the plunger tip to be proximally withdrawn,pulling the retractable needle proximally relative to the needle housingto a retracted state wherein a distal tip of the needle becomesmechanically locked into an encapsulated configuration wherein it is nolonger exposed for injection; and a releasing member operatively coupledto the needle insertion-preventing member, wherein the releasing membercomprises a push member configured to be compressively loaded when theplunger tip is urged into the final insertion state, wherein the needleinsertion-preventing member is configured to prevent re-insertion of theneedle relative to the syringe body after the needle has been placed inthe retracted state, wherein the releasing member is configured toremove a fixing constraint from the insertion-preventing member when theplunger tip reaches the final insertion state, and wherein the pushmember is configured to release a mechanical latch configured to holdthe needle fixed in place relative to the syringe body, therebyreleasing the needle such that it may be proximally withdrawn into theretracted state.
 2. The system of claim 1, wherein the fluid reservoircomprises a substantially cylindrical volume.
 3. The system of claim 1,wherein the syringe body comprises a glass material.
 4. The system ofclaim 1, wherein the syringe body comprises a polymeric material.
 5. Thesystem of claim 1, wherein the plunger tip comprises an elastomericmaterial.
 6. The system of claim 5, wherein the elastomeric materialcomprises a butyl-based rubber.
 7. The system of claim 1, wherein theneedle is a hypodermic needle.
 8. The system of claim 7, wherein thehypodermic needle is a standard size between about 20 gauge and about 34gauge.
 9. The system of claim 1, wherein the insertion-preventing memberis configured to move along an axis that is substantially perpendicularto a longitudinal axis of the needle.
 10. The system of claim 1, whereinthe mechanical latch is configured to interface directly with theneedle.
 11. The system of claim 1, wherein the mechanical latch isconfigured to interface with a needle interfacing member that isinterfaced directly with the needle.
 12. The system of claim 11, whereinthe needle interfacing member comprises a compliant O-ring.
 13. Thesystem of claim 1, wherein the plunger control assembly comprises aplunger tip coupler member configured to be intercoupled with theplunger tip.
 14. The system of claim 13, wherein the plunger tip couplercomprises one or more helical threads configured to be inserted relativeto the plunger tip to couple the plunger tip coupler to the plunger tip.15. The system of claim 13, wherein the plunger tip coupler is fixedlycoupled to a plunger insertion member having a proximal end configuredto be manually manipulated.
 16. The system of claim 15, furthercomprising a plunger guiding flange through which the plunger insertionmember is inserted, the plunger guiding flange being removablycoupleable to the proximal end of the syringe body.
 17. The system ofclaim 16, wherein a brake assembly is intercoupled between the plungerguiding flange and the plunger insertion member, the brake assemblybeing configured to prevent retraction of the plunger insertion memberuntil after the first time it has been inserted to place the plunger tipin the final insertion state.
 18. The system of claim 17, wherein thebrake is configured to reside in a braked state relative to the plungerguiding flange until the plunger insertion member is utilized to placethe plunger tip in the final insertion state, after which the brake isconfigured to mechanically transition to an unbraked state relative tothe plunger guiding flange wherein it is configured to allow the plungerinsertion member to be retracted away from the syringe body.
 19. Thesystem of claim 1, wherein the retraction load is developed by anintegrated spring member.